510(k) K202800 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Pacific Plus PTA Catheter
| Applicant | Medtronic Vascular,Inc(Formerly D.B.A Ev3 Inc.,Covidien, LLC), Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 18, 2020 |
| Received | Sep 23, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202800
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.